Clinical Trial

Refocus VisAbility™ Micro Insert System Pre-market Clinical Trial

Recruiting
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Summary
The primary study objective is to evaluate the safety and effectiveness of the VisAbility™ Micro Insert System for improvement in binocular distance corrected near visual acuity in presbyopic patients.
Trial Details
NCT Number NCT07637500
Lead Sponsor Refocus Group, Inc.
Conditions Presbyopia
Enrollment 33 participants
Start Date 2026-06-02
Primary Completion 2027-12 (estimated)
Study Completion 2027-12 (estimated)
Updated on ClinicalTrials.gov 2026-06-09